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[通过寡核苷酸微阵列分析HG-U133A评估急性心肌梗死患者中与核因子κB(NFκB)相关基因的表达]

[Expression of genes connected with nuclear factor kappa B (NFkappaB) estimated by oligonucleotide microarray analysis HG-U133A in patients with acute myocardial infarction].

作者信息

Dabek Jozefa, Swiderski Robert, Głogowska-Ligus Joanna, Kułach Andrzej, Gasior Zbigniew

机构信息

Slaski Uniwersytet Medyczny w Katowicach, Katedra i Klinika Kardiologii.

出版信息

Pol Merkur Lekarski. 2009 Oct;27(160):265-72.

Abstract

UNLABELLED

Atherosclerosis is a permanently progressive chronic inflammatory disorder which nuclear factor kappaKB (NFkappaB) is involved. Therefore NFkappaB has become integral aspect of atherogenesis and its complications.

THE AIM OF THE STUDY

Estimation of genes expression involved in NFkappaB signaling pathway and separation genes differentiate patients with acute myocardial infarction from healthy subjects.

MATERIAL AND METHODS

The examination was assess using the Affymetrix HG-U133A oligonucleotide microarray. Differentiating genes were determined using Bland-Altman graph analysis. Patients wasn't treated due to cardiac diseases before. All patients were subjected to 12-lead ECG, 2-D echocardiography, coronarography and laboratory studies including cardiac troponin, CK and CK-MB. The healthy individuals were subjected to coronarography and computed tomography (calcium score)--coronary artery disease was out of the question.

RESULTS

Hierarchical clusterization has demonstrated that the genes expression of patients with acute myocardial infarction was different from healthy individuals. It also demonstrated that the individual groups are homogeneous, especially the group of patients with acute myocardial infarction, regardless of diagnosis, number of risk factors and progression of coronary artery disease. Further Bland-Altman graph analysis showed three important differentiating genes: TLR2, TNFRSF1A i IKBKAP.

CONCLUSIONS

Our results confirmed the share of genes involved in NFkappaB signaling pathway in acute complications of atherosclerosis. Noticed differences in genes expression of patients with acute myocardial infarction and healthy subjects can show important role isolated differentiating genes in destabilization of atherogenic plaque and acute myocardial infarction occurrence.

摘要

未标注

动脉粥样硬化是一种核因子κB(NFκB)参与其中的永久性进行性慢性炎症性疾病。因此,NFκB已成为动脉粥样硬化及其并发症的一个不可或缺的方面。

研究目的

评估参与NFκB信号通路的基因表达,并分离出能区分急性心肌梗死患者与健康受试者的基因。

材料与方法

使用Affymetrix HG-U133A寡核苷酸微阵列进行检测。使用布兰德-奥特曼图分析确定差异基因。患者此前未因心脏病接受过治疗。所有患者均接受了12导联心电图、二维超声心动图、冠状动脉造影以及包括心肌肌钙蛋白、肌酸激酶和肌酸激酶同工酶在内的实验室检查。健康个体接受了冠状动脉造影和计算机断层扫描(钙化评分)——冠状动脉疾病不在考虑范围内。

结果

层次聚类分析表明,急性心肌梗死患者的基因表达与健康个体不同。它还表明各个组是同质的,尤其是急性心肌梗死患者组,无论诊断、危险因素数量和冠状动脉疾病进展情况如何。进一步的布兰德-奥特曼图分析显示了三个重要的差异基因:TLR2、TNFRSF1A和IKBKAP。

结论

我们的结果证实了参与NFκB信号通路的基因在动脉粥样硬化急性并发症中的作用。急性心肌梗死患者与健康受试者基因表达的明显差异表明,分离出的差异基因在动脉粥样硬化斑块不稳定和急性心肌梗死发生中具有重要作用。

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